Caire recalls Liberator 30 liquid oxygen units with model 13337403 due to potential weld issues. Affected units have specific serial numbers and UDI codes. Consumers should check their units and contact Caire for details.
An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.
Caire is recalling some Liberator 30 liquid oxygen systems because an audit found welding inconsistencies in the inner bottle. This could lead to leaks or failures if the welds are weak, but the recall doesn't specify immediate danger to users.
The audit found some units have inconsistent weld penetration on the inner bottle's longitudinal weld seam. This could cause leaks or failures if the welds are weak, but the recall doesn't specify immediate danger to users.
Users of the Caire Liberator 30 liquid oxygen system with model number 13337403 are affected. Those who use the device for medical oxygen therapy are most at risk due to potential leaks.
Check for the model number 13337403 on the device. Affected units have specific serial numbers: CBB3022300368, CBB3022300390, CBB3022300470, CBB3022300472, CBB3022300479. The UDI code is M766133374030.
Look for the model number 13337403 and the listed serial numbers on your device.
An audit discovered some units have inconsistencies in weld penetration on the inner bottle's longitudinal weld seam.
Check your unit for the model number 13337403 and the listed serial numbers. Contact Caire for further instructions.
The recall indicates potential weld issues that could lead to leaks or failures, but the record doesn't specify immediate danger to users.
We’ve drafted a message you can send Caire to request your refund or repair — edit it as you like.
Subject: Recall Z-0338-2023 — Caire Caire Hello, I own a Caire that is covered by recall Z-0338-2023 from Caire. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
